POLYCRYSTALLINE ZnO NANOWIRES OBTAINED BY PYROLIZING ZINC OXALATE-BASED NANOWIRES FROM TEMPLATE-ASSISTED SOLUTIONS

2011 ◽  
Vol 10 (03) ◽  
pp. 471-478 ◽  
Author(s):  
DONG-HAU KUO ◽  
HSIANG CHANG ◽  
JU-YIN CHENG

Polycrystalline ZnO nanowires composed of nanosized grains were produced by pyrolizing one-dimensional (1D) zinc oxalate-based nanowires at 450°C. The oxalate-based nanowires were synthesized at 25°C–100°C in an aqueous solution with the aid of a hexamethyleneamide (HMA) template and catalytic ammonia. Due to its low solubility in aqueous solution, zinc oxalate was not the popular reactant for the synthesis of ZnO . With a fixed ammonia concentration and a HMA/[ ZnC2O4 ⋅ H2O ] molar ratio of 1, the growth of zinc oxalate-based wires was investigated by changing growth temperature and growth duration. Different growth behaviors were observed and explained based upon the decomposition rate of [Formula: see text] complex and the interaction between zinc oxalate molecules and surfactants. The best growth condition was at 80°C for less than 1 h. After low-temperature calcination at 450°C, zinc oxalate-based nanowires were pyrolized into polycrystalline ZnO nanowires. This synthesis provides a simple route to prepare nanoparticle-covered ZnO nanowires.

Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3358
Author(s):  
Sadaf Rauf ◽  
Agata Trzesowska-Kruszynska ◽  
Tomasz Sierański ◽  
Marcin Świątkowski

Three new copper coordination compounds derived from 2,2-bis(hydroxymethyl)propionic acid (dmpa) and hexamethylenetetramine (hmta) were obtained and their crystal structures were determined. The stoichiometry of the reagents applied in the syntheses reflects the metal to ligand molar ratio in the formed solid products. Due to the multiple coordination modes of the used ligands, wide structural diversity was achieved among synthesized compounds, i.e., mononuclear [Cu(dmp)2(hmta)2(H2O)] (1), dinuclear [Cu2(dmp)4(hmta)2] (2), and 1D coordination polymer [Cu2(dmp)4(hmta)]n (3). Their supramolecular structures are governed by O—H•••O and O—H•••N hydrogen bonds. The compounds were characterized in terms of absorption (UV-Vis and IR) and thermal properties. The relationships between structural features and properties were discussed in detail. Owing to discrepancies in the coordination mode of a dmp ligand, bidentate chelating in 1, and bidentate bridging in 2 and 3, there is a noticeable change in the position of the bands corresponding to the stretching vibrations of the carboxylate group in the IR spectra. The differences in the structures of the compounds are also reflected in the nature and position of the UV-Vis absorption maxima, which are located at lower wavelengths for 1.


2020 ◽  
Vol 20 (8) ◽  
pp. 5019-5033 ◽  
Author(s):  
Yuning Xie ◽  
Gehui Wang ◽  
Xinpei Wang ◽  
Jianmin Chen ◽  
Yubao Chen ◽  
...  

Abstract. The Chinese government has exerted strict emission controls to mitigate air pollution since 2013, which has resulted in significant decreases in the concentrations of air pollutants such as SO2. Strict pollution control actions also reduced the average PM2.5 concentration to the low level of 39.7 µg m−3 in urban Beijing during the winter of 2017. To investigate the impact of such changes on the physiochemical properties of atmospheric aerosols in China, we conducted a comprehensive observation focusing on PM2.5 in Beijing during the winter of 2017. Compared with the historical record (2014–2017), SO2 decreased to the low level of 3.2 ppbv in the winter of 2017, but the NO2 level was still high (21.4 ppbv in the winter of 2017). Accordingly, the contribution of nitrate (23.0 µg m−3) to PM2.5 far exceeded that of sulfate (13.1 µg m−3) during the pollution episodes, resulting in a significant increase in the nitrate-to-sulfate molar ratio. The thermodynamic model (ISORROPIA II) calculation results showed that during the PM2.5 pollution episodes particle pH increased from 4.4 (moderate acidic) to 5.4 (more neutralized) when the molar ratio of nitrate to sulfate increased from 1 to 5, indicating that aerosols were more neutralized as the nitrate content elevated. Controlled variable tests showed that the pH elevation should be attributed to nitrate fraction increase other than crustal ion and ammonia concentration increases. Based on the results of sensitivity tests, future prediction for the particle acidity change was discussed. We found that nitrate-rich particles in Beijing at low and moderate humid conditions (RH: 20 %–50 %) can absorb twice the amount of water that sulfate-rich particles can, and the nitrate and ammonia with higher levels have synergetic effects, rapidly elevating particle pH to merely neutral (above 5.6). As moderate haze events might occur more frequently under abundant ammonia and nitrate-dominated PM2.5 conditions, the major chemical processes during haze events and the control target should be re-evaluated to obtain the most effective control strategy.


2015 ◽  
Vol 71 (11) ◽  
pp. 1384-1387
Author(s):  
Marwen Chouri ◽  
Habib Boughzala

The title compound bis(1,4-diazoniabicyclo[2.2.2]octane) di-μ-chlorido-bis[tetrachloridobismuthate(III)] dihydrate, (C6H14N2)2[Bi2Cl10]·2H2O, was obtained by slow evaporation at room temperature of a hydrochloric aqueous solution (pH = 1) containing bismuth(III) nitrate and 1,4-diazabicyclo[2.2.2]octane (DABCO) in a 1:2 molar ratio. The structure displays a two-dimensional arrangement parallel to (100) of isolated [Bi2Cl10]4−bioctahedra (site symmetry -1) separated by layers of organic 1,4-diazoniabicyclo[2.2.2]octane dications [(DABCOH2)2+] and water molecules. O—H...Cl, N—H...O and N—H...Cl hydrogen bonds lead to additional cohesion of the structure.


2003 ◽  
Vol 788 ◽  
Author(s):  
Andrei A. Eliseev ◽  
Kirill S. Napolskii ◽  
Dmitry F. Gorozhankin ◽  
Alexei V. Lukashin ◽  
Yuri D. Tretyakov ◽  
...  

ABSTRACTHere we report the synthesis and investigation of iron and iron oxide nanowire arrays using mesoporous silica as a host material. In the present work a novel variant of synthesis of ordered magnetic nanowires in the mesoporous silica matrix was suggested. The method is based on the incorporation of a hydrophobic metal compound into the hydrophobic part of silica-surfactant composite. The amount of iron intercalated into the mesoporous matrix was measured by chemical analysis. In all samples it corresponds well to with the molar ratio SiO2: Fe = 9:1. To provide crystallinity of nanowires additional thermal treatment was performed. Thus prepared nanocomposites were characterized by TEM, ED, SAXS, SANS, BET and magnetic measurements. The anisotropy parameters of nanowires were determined using two non-correlated methods: temperature dependence of magnetic susceptibility and small angle polarized neutron scattering. It was found that the particle length increases with the increasing of the decomposition temperature of the metal complex. Obviously it deals with crystallization and growth of metal particles inside the pores at a constant diameter of a single particle. For iron containing sample annealed at 375 °C (form factor of nanowire is about 40), the coercive force at room temperature was found to be 145 Oe at saturation magnetization of 1.2 emu/g, which is not far from modern information storage. It was shown that particles shape and size are in good agreement with that of the pores. Particles are uniform and well ordered in the silica matrix. Thus, the suggested method leads to one-dimensional anisotropic nanostructures which could find an application as high-density data storage magnetic media.


2005 ◽  
Vol 24 (1_suppl) ◽  
pp. 103-117 ◽  

Potassium Silicate, Sodium Metasilicate, and Sodium Silicate combine metal cations with silica to form inorganic salts used as corrosion inhibitors in cosmetics. Sodium Metasilicate also functions as a chelating agent and Sodium Silicate as a buffering and pH adjuster. Sodium Metasilicate is currently used in 168 formulations at concentrations ranging from 13% to 18%. Sodium Silicate is currently used in 24 formulations at concentrations ranging from 0.3% to 55%. Potassium Silicate and Sodium Silicate have been reported as being used in industrial cleaners and detergents. Sodium Metasilicate is a GRAS (generally regarded as safe) food ingredient. Aqueous solutions of Sodium Silicate species are a part of a chemical continuum of silicates based on an equilibrium of alkali, water, and silica. pH determines the solubility of silica and, together with concentration, determines the degree of polymerization. Sodium Silicate administered orally is readily absorbed from the alimentary canal and excreted in the urine. The toxicity of these silicates has been related to the molar ratio of SiO2/Na2O and the concentration being used. The Sodium Metasilicate acute oral LD50 ranged from 847 mg/kg in male rats to 1349.3 mg/kg in female rats and from 770 mg/kg in female mice to 820 mg/kg in male mice. Gross lesions of variable severity were found in the oral cavity, pharynx, esophagus, stomach, larynx, lungs, and kidneys of dogs receiving 0.25 g/kg or more of a commercial detergent containing Sodium Metasilicate; similar lesions were also seen in pigs administered the same detergent and dose. Male rats orally administered 464 mg/kg of a 20% solution containing either 2.0 or 2.4 to 1.0 ratio of sodium oxide showed no signs of toxicity, whereas doses of 1000 and 2150 mg/kg produced gasping, dypsnea, and acute depression. Dogs fed 2.4 g/kg/day of Sodium Silicate for 4 weeks had gross renal lesions but no impairment of renal function. Dermal irritation of Potassium Silicate, Sodium Metasilicate, and Sodium Silicate ranged from negligible to severe, depending on the species tested and the molar ratio and concentration tested. Sodium Metasilicate was negative in the local lymph node assay (LLNA), but a delayed-type hypersensitivity response was observed in mice. Potassium Silicate was nonirritating in two acute eye irritation studies in rabbits. Sodium Metasilicate (42.4% H20) was corrosive to the rabbit eye. Sodium Silicate was a severe eye irritant in some eye irritation studies, but was irritating or nonirritating in others. A skin freshener containing Sodium Silicate was nonirritating. Sodium Metasilicate was nonmutagenic in bacterial cells. Rats given Sodium Silicate (600 and 1200 ppm of added silica) in the drinking water in reproductive studies produced a reduced number of offspring: to 67% of controls at 600 ppm and to 80% of controls at 1200 ppm. Three adult rats injected intratesticularly and subcutaneously with 0.8 mM/kg of Sodium Silicate showed no morphological changes in the testes and no effect on the residual spermatozoa in the ductus deferens. Sodium Metasilicate (37% in a detergent) mixed with water was a severe skin irritant when tested on intact and abraded human skin, but 6%, 7%, and 13% Sodium Silicate were negligible skin irritants to intact and abraded human skin. Sodium Silicate (10% of a 40% aqueous solution) was negative in a repeat-insult predictive patch test in humans. The same aqueous solution of Sodium Silicate was considered a mild irritant under normal use conditions in a study of cumulative irritant properties. The Cosmetic Ingredient Review (CIR) Expert Panel recognized the irritation potential of these ingredients, especially in leave-on products. However, because these ingredients have limited dermal absorption and Sodium Metasilicate is a GRAS direct food substance, the Panel deemed the ingredients safe for use in cosmetic products in the practices of use and concentration described in this safety assessment, when formulated to avoid irritation.


2011 ◽  
Vol 239-242 ◽  
pp. 3337-3341
Author(s):  
Dong Xia Zhang ◽  
Wen Hui Hu ◽  
Fang Ping Wang ◽  
Lin Ke Xue ◽  
Xin Zhen Du

An amphiphilic graft copolymer with poly(acrylamide-methacrylate) as a main chain and octylphenyl polyoxyethylene as side chains (P(AM-MA)-g-C8PhEO10) was successfully synthesized via free radical copolymerization. The structure and the composition of the graft copolymer were characterized by FTIR, 1H-NMR and elemental analysis (EA) in detail. The absolute molecular weight of the copolymer is 1.304×106, as determined by static light scattering (SLS). The molar ratio of acrylamide monomer to the macromonomer is 33:1 in the copolymer and 53 C8PhEO10 branch chains attach to a P(AM-MA) backbone. The micellar behavior of P(AM-MA)-g-C8PhEO10 was preliminarily studied by means of surface tension measurements, transmission electron microscope (TEM) in aqueous solution. It was found that the stable spherical micelles with core-shell structure are formed and polymolecular micelles are larger and more compact than monomolecular micelles. In addition, the graft copolymer has favorable thermal stability.


Materials ◽  
2019 ◽  
Vol 12 (11) ◽  
pp. 1864 ◽  
Author(s):  
Ziling Cao ◽  
Chen Zhang ◽  
Zhuoxin Yang ◽  
Qing Qin ◽  
Zhihua Zhang ◽  
...  

Carbon aerogel (CA) has a rich porous structure, in which micropores and mesopores provide a huge specific surface area to form electric double layers. This property can be applied to the application of capacitive deionization (CDI). The adsorption effect of CA electrode on Cu2+ in an aqueous solution was explored for solving heavy metal water pollution. The CAs were synthesized by a sol-gel process using an atmospheric drying method. The structure of CAs was characterized by scanning in an electron microscope (SEM) and nitrogen adsorption/desorption techniques. The adsorption system was built using Cu2+ solution as the simulation of heavy metal pollution solution. The control variate method was used to investigate the effect of the anion species in copper solution, the molar ratio of resorcinol to catalyst (R/C) of CA, and the applied voltage and concentration of copper ion on the adsorption results.


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